Nonaqueous-electrolyte secondary battery and secondary battery module

ABSTRACT

A secondary battery module includes a nonaqueous-electrolyte secondary battery and an elastic body, wherein a negative electrode constituting the nonaqueous-electrolyte secondary battery includes a negative-electrode active material layer, the negative-electrode active material layer includes a first layer, and a second layer that is formed on the first layer and has a higher compression modulus than the first layer, a separator constituting the nonaqueous-electrolyte secondary battery has a lower compression modulus than the first layer, the elastic body has a lower compression modulus than the separator, the graphite particles contained in the first layer have a BET specific surface area of 1 to 2.5 m 2 /g, and the content of Si particles in the first layer is 6 mass % to 13 mass % relative to the total amount of the negative-electrode active material layer.

CROSS REFERENCE TO RELATED APPLICATION

The entire disclosure of Japanese Patent Application No. 2020-021759filed on Feb. 12, 2020 including the specification, claims, drawings,and abstract is incorporated herein by reference in its entirety.

TECHNICAL FIELD

The present disclosure generally relates to a technique of anonaqueous-electrolyte secondary battery and a secondary battery module.

BACKGROUND

A nonaqueous-electrolyte secondary battery, e.g., a lithium-ionsecondary battery, is typically provided with an electrode body in whicha positive electrode including a positive-electrode active materiallayer and a negative electrode including a negative-electrode activematerial layer are stacked with a separator interposed therebetween, andan electrolytic solution. Such a nonaqueous-electrolyte secondarybattery is, for example, a battery that is charged and discharged bycharge carriers (e.g., lithium ions) moving between electrodes in anelectrolytic solution. During the charge of the nonaqueous-electrolytesecondary battery, charge carriers are released from thepositive-electrode active material constituting the positive-electrodeactive material layer and are occluded into the negative-electrodeactive material constituting the negative-material active materiallayer. During the discharge, conversely, charge carriers are releasedfrom the negative-electrode active material and are occluded into thepositive-electrode active material. In this way, when charge carriersare occluded and released into and from the active materials during thecharge and discharge of the nonaqueous-electrolyte secondary battery,the electrode body expands and contracts.

If the expansion and contraction of the electrode body in response tothe charge and discharge of the nonaqueous-electrolyte secondary batterypresses an electrolytic solution stored in the electrode body out of theelectrode body, unfortunately, a battery resistance may increase duringhigh-rate charge and discharge.

For example, Patent Document 1 proposes a secondary battery in which anegative electrode has a higher compression modulus than a separator.Furthermore, Patent Document 1 discloses that a negative electrode has ahigher compression modulus than a separator and thus the retainabilityof an electrolytic solution in an electrode body is improved and anincrease in battery resistance is suppressed, particularly when chargeand discharge are repeated at a high rate.

Moreover, it is conventionally known that Si materials such as lithiumsilicate (Li_(x)SiO_(y)) can occlude many lithium ions per unit volumeas compared with carbon active materials such as graphite (for example,see Patent Document 2). Thus, using an Si material as anegative-electrode active material can increase the capacity of thenonaqueous-electrolyte secondary battery.

CITATION LIST Patent Literature

Patent Document 1: JP 6587105 B

Patent Document 2: WO 2019/187537 A

SUMMARY Technical Problem

However, the nonaqueous-electrolyte secondary battery containing an Simaterial as a negative-electrode active material is likely to decreasein capacity recovery rate after being stored at high temperature.

It is an advantage of the present disclosure to suppress an increase inresistance during high-rate charge and discharge and a reduction incapacity recovery rate after high-temperature storage, in anonaqueous-electrolyte secondary battery containing negative-electrodeactive materials including an Si material and a secondary battery moduleincluding the nonaqueous-electrolyte secondary battery.

Solution to Problem

A secondary battery module according to an aspect of the presentdisclosure is a secondary battery module comprising: at least onenonaqueous-electrolyte secondary battery, and an elastic body that isplaced with the nonaqueous-electrolyte secondary battery and receives aload from the nonaqueous-electrolyte secondary battery in the placementdirection of the elastic body, wherein the nonaqueous-electrolytesecondary battery includes an electrode body in which a positiveelectrode, a negative electrode, and a separator disposed between thepositive electrode and the negative electrode are stacked, and a housingaccommodating the electrode body; the negative electrode includes anegative-electrode current collector and a negative-electrode activematerial layer that is formed on the negative-electrode currentcollector and contains negative-electrode active material particles, thenegative-electrode active material layer including a first layer formedon the negative-electrode current collector, and a second layer that isformed on the first layer and has a higher compression modulus than thefirst layer, the separator has a lower compression modulus than thefirst layer, the elastic body has a lower compression modulus than theseparator, the negative-electrode active material particles contained inthe first layer include graphite particles and at least one Si particleselected from the group consisting of lithium silicate particles andsilicon carbon composite particles, the graphite particles contained inthe first layer have a BET specific surface area of 1 to 2.5 m²/g, andthe content of the Si particles is 6 mass % to 13 mass % relative to thetotal amount of the negative-electrode active material layer.

A nonaqueous-electrolyte secondary battery according to an aspect of thepresent disclosure is a nonaqueous-electrolyte secondary batteryincluding an electrode body in which a positive electrode, a negativeelectrode, and a separator disposed between the positive electrode andthe negative electrode are stacked, an elastic body configured toreceive a load from the electrode body in the stacking direction of theelectrode body, and a housing accommodating the electrode body and theelastic body, wherein the negative electrode includes anegative-electrode current collector and a negative-electrode activematerial layer that is formed on the negative-electrode currentcollector and contains negative-electrode active material particles, thenegative-electrode active material layer including a first layer formedon the negative-electrode current collector, and a second layer that isformed on the first layer and has a higher compression modulus than thefirst layer, the separator has a lower compression modulus than thefirst layer, the elastic body has a lower compression modulus than theseparator, the negative-electrode active material particles contained inthe first layer include graphite particles and at least one Si particleselected from the group consisting of lithium silicate particles andsilicon carbon composite particles, the graphite particles contained inthe first layer have a BET specific surface area of 1 to 2.5 m²/g, andthe content of the Si particles is 6 mass % to 13 mass % relative to thetotal amount of the negative-electrode active material layer.

Advantageous Effect of Invention

An aspect of the present disclosure can suppress an increase inresistance during high-rate charge and discharge and a reduction incapacity recovery rate after high-temperature storage.

BRIEF DESCRIPTION OF DRAWINGS

Embodiment(s) of the present disclosure will be described based on thefollowing figures, wherein:

FIG. 1 is a perspective view illustrating a secondary battery moduleaccording to an embodiment;

FIG. 2 is an exploded perspective view illustrating the secondarybattery module according to the embodiment;

FIG. 3 is a schematic cross-sectional view of expandingnonaqueous-electrolyte secondary batteries;

FIG. 4 is a schematic cross-sectional view of the negative electrode;

FIG. 5 is a schematic cross-sectional view of elastic bodies disposed ina housing;

FIG. 6 is a schematic perspective view illustrating an electrode body ofa cylindrical winding type;

FIG. 7 is a schematic perspective view illustrating an example of theelastic body; and

FIG. 8 is a partial schematic cross-sectional view of the elastic bodydisposed between the electrode body and the housing.

DESCRIPTION OF EMBODIMENT

An example of an embodiment will be specifically described below.Drawings to be referred in the description of the embodiment areschematically illustrated and thus the dimensional ratios or the like ofconstituent elements illustrated in the drawings may be different fromthose of an actual configuration.

FIG. 1 is a perspective view illustrating a secondary battery moduleaccording to the embodiment. FIG. 2 is an exploded perspective viewillustrating the secondary battery module according to the embodiment. Asecondary battery module 1 includes, for example, a stack 2, a pair oflocking members 6, and a cooling plate 8. The stack 2 includes aplurality of nonaqueous-electrolyte secondary batteries 10, a pluralityof insulating spacers 12, a plurality of elastic bodies 40, and a pairof end plates 4.

The nonaqueous-electrolyte secondary batteries 10 are secondarybatteries that can be charged and discharged, such as lithium-ionsecondary batteries. The nonaqueous-electrolyte secondary battery 10 ofthe present embodiment is a so-called rectangular battery including anelectrode body 38 (see FIG. 3), an electrolytic solution, and a housing13 shaped like a flat rectangular prism. The housing 13 includes anouter can 14 and a sealing plate 16. The outer can 14 has asubstantially rectangular opening on one surface. The electrode body 38and an electrolytic solution or the like are stored in the outer can 14through the opening. The outer can 14 is desirably coated with aninsulating film, e.g., a shrink tube, which is not illustrated. Thesealing plate 16 for closing the opening and sealing the outer can 14 isprovided on the opening of the outer can 14. The sealing plate 16constitutes a first surface 13 a of the housing 13. The sealing plate 16and the outer can 14 are joined to each other by, for example, laser,friction stir welding, or brazing and soldering.

The housing 13 may be, for example, a cylindrical case or an exteriorpart composed of a laminated sheet including a metallic layer and aresin layer.

The electrode body 38 is configured such that a plurality of sheetpositive electrodes 38 a and a plurality of sheet negative electrodes 38b are alternately stacked with separators 38 d, each being interposedbetween adjacent positive electrodes 38 a and negative electrodes 38 b(see FIG. 3). The positive electrodes 38 a, the negative electrodes 38b, and the separators 38 d are stacked in a first direction X. In otherwords, the first direction X is the stacking direction of the electrodebodies 38. Moreover, the electrodes on both ends in the stackingdirection face the long lateral faces of the housing 13. The longlateral faces will be described later. The first direction X, a seconddirection Y, and a third direction Z in the drawings are orthogonal toone another.

The electrode body 38 may be an electrode body of a cylindrical windingtype, in which a strip positive electrode and a strip negative electrodeare stacked with a separator interposed therebetween, or an electrodebody of a flat winding type that is formed by flattening an electrodebody of a cylindrical winding type. For an electrode body of the flatwinding type, an outer can resembling a rectangular prism may be used.For an electrode body of the cylindrical winding type, a cylindricalouter can is used.

On the sealing plate 16; that is, on the first surface 13 a of thehousing 13, an output terminal 18 is provided on one end in thelongitudinal direction while being electrically connected to thepositive electrode 38 a of the electrode body 38, and an output terminal18 is provided on the other end while being electrically connected tothe negative electrode 38 b of the electrode body 38. Hereinafter, theoutput terminal 18 connected to the positive electrode 38 a will bereferred to as a positive terminal 18 a, and the output terminal 18connected to the negative electrode 38 b will be referred to as anegative terminal 18 b. When it is not necessary to discriminate betweenthe polarities of the pair of the output terminals 18, the positiveterminal 18 a and the negative terminal 18 b are collectively referredto as the output terminals 18.

The outer can 14 has a bottom opposed to the sealing plate 16. The outercan 14 also has four lateral faces connecting the opening and thebottom. Two of the four lateral faces are a pair of long lateral facesconnected to two opposed long sides of the opening. The long lateralfaces are surfaces having the largest area among the faces of the outercan 14; that is, main surfaces. Moreover, the long lateral faces arelateral faces extending in a direction crossing (for example, orthogonalto) the first direction X. Two lateral faces other than the two longlateral faces are a pair of short lateral faces connected to the openingand the short sides of the bottom of the outer can 14. The bottom, longlateral faces, and short lateral faces of the outer can 14 correspondrespectively to the bottom, long lateral faces, and short lateral facesof the housing 13.

In the description of the present embodiment, for convenience, the firstsurface 13 a of the housing 13 is illustrated as the top surface of thenonaqueous-electrolyte secondary battery 10. Furthermore, the bottom ofthe housing 13 corresponds to the bottom of the nonaqueous-electrolytesecondary battery 10, the long lateral faces of the housing 13correspond to the long lateral faces of the nonaqueous-electrolytesecondary battery 10, and the short lateral faces of the housing 13correspond to the short lateral faces of the nonaqueous-electrolytesecondary battery 10. The secondary battery module 1 has a top surfacenear the top surfaces of the nonaqueous-electrolyte secondary batteries10, a bottom near the bottoms of the nonaqueous-electrolyte secondarybatteries 10, and lateral faces near the short lateral faces of thenonaqueous-electrolyte secondary batteries 10. Moreover, the top surfaceof the secondary battery module 1 is located on the upper side in avertical direction and the bottom of the secondary battery module 1 islocated on the lower side in the vertical direction.

The nonaqueous-electrolyte secondary batteries 10 are provided inparallel at predetermined intervals such that the long lateral faces ofthe adjacent nonaqueous-electrolyte secondary batteries 10 are opposedto each other. Furthermore, in the present embodiment, the outputterminals 18 of the nonaqueous-electrolyte secondary batteries 10 areoriented in the same direction. The output terminals 18 may be orientedin different directions.

The two adjacent nonaqueous-electrolyte secondary batteries 10 arearranged (placed) such that the positive terminal 18 a of one of thenonaqueous-electrolyte secondary batteries 10 and the negative terminal18 b of the other nonaqueous-electrolyte secondary battery 10 areadjacent to each other. The positive terminal 18 a and the negativeterminal 18 b are connected in series via a bus bar (not illustrated).Alternatively, the output terminals 18 with the same polarity on theadjacent nonaqueous-electrolyte secondary batteries 10 may be connectedin parallel via a bus bar so as to form nonaqueous-electrolyte secondarybattery blocks, and the nonaqueous-electrolyte secondary battery blocksmay be connected in series.

The insulating spacer 12 is disposed between the two adjacentnonaqueous-electrolyte secondary batteries 10 and provides electricalinsulation between the two nonaqueous-electrolyte secondary batteries10. The insulating spacer 12 is made of, for example, insulating resin.The insulating spacer 12 is made of resins including, for example,polypropylene, polybutylene terephthalate, and polycarbonate. Thenonaqueous-electrolyte secondary batteries 10 and the insulating spacers12 are alternately placed. The insulating spacer 12 is also disposedbetween the nonaqueous-electrolyte secondary battery 10 and the endplate 4.

The insulating spacer 12 has a flat part 20 and a wall part 22. The flatpart 20 is interposed between the opposed long lateral faces of the twoadjacent nonaqueous-electrolyte secondary batteries 10. This ensuresinsulation between the outer cans 14 of the adjacentnonaqueous-electrolyte secondary batteries 10.

The wall part 22 extends from the outer edge of the flat part 20 in thedirection of arranging the nonaqueous-electrolyte secondary batteries 10and covers a part of the top surface, the lateral face, and a part ofthe bottom of the nonaqueous-electrolyte secondary battery 10. This can,for example, obtain a lateral-face distance between the adjacentnonaqueous-electrolyte secondary batteries 10 or between thenonaqueous-electrolyte secondary battery 10 and the end plate 4. Thewall part 22 has a notch 24 where the bottom of thenonaqueous-electrolyte secondary battery 10 is exposed. The insulatingspacer 12 has urge receiving portions 26 that are placed face up at eachend of the insulating spacer 12 in the second direction Y.

The elastic bodies 40 are placed with the nonaqueous-electrolytesecondary batteries 10 along the first direction X. In other words, thefirst direction X is, as described above, the stacking direction of theelectrode bodies 38 and is also the placement direction of thenonaqueous-electrolyte secondary batteries 10 and the elastic bodies 40.The elastic body 40 is a sheet member disposed between the long lateralface of the nonaqueous-electrolyte secondary battery 10 and the flatpart 20 of the insulating spacer 12, for example. The elastic body 40disposed between the two adjacent nonaqueous-electrolyte secondarybatteries 10 may be a sheet or a stack of a plurality of stacked sheets.The elastic body 40 may be fixed to the surface of the flat part 20 withadhesive or the like. Alternatively, the flat part 20 may have arecessed portion and the elastic body 40 may be fit into the recessedportion. Furthermore, the elastic body 40 and the insulating spacer 12may be molded in one piece. Moreover, the elastic body 40 may be used asthe flat part 20. The structure and effects of the elastic body 40 willbe specifically discussed later.

The nonaqueous-electrolyte secondary batteries 10, the insulatingspacers 12, and the elastic bodies 40 that are provided in parallel aresandwiched between the pair of end plates 4 in the first direction X.The end plate 4 includes, for example, a metallic plate or a resinplate. The end plate 4 has screw holes 4 a that penetrate the end plate4 in the first direction X and into which screws 28 are to be inserted.

The pair of locking members 6 are long members that are longitudinallyextended in the first direction X. The pair of locking members 6 areopposed to each other in the second direction Y. The stack 2 is disposedbetween the pair of locking members 6. The locking member 6 includes abody portion 30, a support portion 32, a plurality of urging portions34, and a pair of fixing portions 36.

The body portion 30 is a rectangular portion extending in the firstdirection X. The body portion 30 extends in parallel with the lateralfaces of the nonaqueous-electrolyte secondary batteries 10. The supportportion 32 extends in the first direction X and protrudes from the lowerend of the body portion 30 in the second direction Y. The supportportion 32 is a continuous plate member that extends in the firstdirection X and supports the stack 2.

The urging portions 34 are connected to the upper end of the bodyportion 30 and protrude in the second direction Y. The support portion32 and the urging portions 34 are opposed to each other in the thirddirection Z. The urging portions 34 are placed at predeterminedintervals in the first direction X. The urging portions 34 are shapedlike, for example, leaf springs that urge the nonaqueous-electrolytesecondary batteries 10 to the support portion 32.

The pair of fixing portions 36 are plate members that protrude in thesecond direction Y from both ends of the body portion 30 in the firstdirection X. The pair of fixing portions 36 are opposed to each other inthe first direction X. The fixing portion 36 has through holes 36 awhere the screws 28 are inserted. The pair of fixing portions 36 fix thelocking members 6 to the stack 2.

The cooling plate 8 is a mechanism for cooling thenonaqueous-electrolyte secondary batteries 10. The stack 2 locked by thepair of locking members 6 is placed on the major surface of the coolingplate 8 and is fixed to the cooling plate 8 by inserting fasteningmembers (not illustrated) such as screws into through holes 32 a of thesupport portion 32 and through holes 8 a of the cooling plate 8.

FIG. 3 is a schematic cross-sectional view of the expandingnonaqueous-electrolyte secondary batteries. The number ofnonaqueous-electrolyte secondary batteries 10 is reduced in theillustration of FIG. 3. Moreover, the illustration of the internalstructures of the nonaqueous-electrolyte secondary batteries 10 issimplified and the insulating spacers 12 are omitted. As illustrated inFIG. 3, the electrode body 38 (the positive electrodes 38 a, thenegative electrodes 38 b, the separators 38 d) is stored in each of thenonaqueous-electrolyte secondary batteries 10. The outer can 14 of thenonaqueous-electrolyte secondary battery 10 expands and contractsaccording to the expansion and contraction of the electrode body 38during charge and discharge. The expansion of the outer can 14 of thenonaqueous-electrolyte secondary battery 10 generates a load G1 that isapplied outward in the first direction X in the stack 2. In other words,the elastic bodies 40 placed with the nonaqueous-electrolyte secondarybatteries 10 receive loads from the nonaqueous-electrolyte secondarybatteries 10 in the first direction X (the placement direction of thenonaqueous-electrolyte secondary batteries 10 and the elastic bodies40). To the stack 2, a load G2 correspond to the load G1 is applied bythe locking member 6.

The compression moduli of the negative electrode 38 b, the separator 38d, and the elastic body 40 will be described below.

FIG. 4 is a schematic cross-sectional view of the negative electrode. Asillustrated in FIG. 4, the negative electrode 38 b includes anegative-electrode current collector 50 and a negative-electrode activematerial layer 52 that is disposed on the negative-electrode currentcollector 50 and contains negative-electrode active material particles.The negative-electrode active material layer 52 includes a first layer52 a formed on the negative-electrode current collector 50 and a secondlayer 52 b formed on the first layer 52 a. The second layer 52 b has ahigher compression modulus than the first layer 52 a. In other words,the negative-electrode active material layer 52 has a high compressionmodulus near the surface and has a low compression modulus near thenegative-electrode current collector. Furthermore, the separator 38 dhas a lower compression modulus than the first layer 52 a. The elasticbody 40 has a lower compression modulus than the separator 38 d. Inother words, the compression modulus decreases in the order of thesecond layer 52 b near the surface>the first layer 52 a near thenegative-electrode current collector>the separator 38 d>the elastic body40. Thus, in this configuration, the second layer 52 b near the surfaceis the most resistant to deformation and the elastic body 40 is the mostdeformable. As described above, the present embodiment specifies thecompression moduli of the members, thereby suppressing an increase inresistance during high-rate charge and discharge. This mechanism is notsufficiently identified but is assumed to be configured as follows:

Typically, the electrode body 38 expands and contracts in response tothe charge and discharge of the nonaqueous-electrolyte secondary battery10, thereby pressing an electrolytic solution in the electrode body 38out of the electrode body 38. In the present embodiment, however, thesecond layer 52 b near the surface of the negative-electrode activematerial layer 52 has a large compression modulus, thereby suppressingthe expansion and contraction of the second layer 52 b when thenonaqueous-electrolyte secondary battery 10 is charged or discharged.Furthermore, the compression of the second layer 52 b is absorbed by thefirst layer 52 a having a lower compression modulus than the secondlayer 52 b (in other words, the first layer 52 a is more deformable thanthe second layer 52 b). Moreover, the expansion and contraction of thefirst layer 52 a on the current-collector side of the negative-electrodeactive material layer 52 are absorbed by the separator 38 d having alower compression modulus than the first layer 52 a (in other words, theseparator 38 d is more deformable than the first layer 52 a). Thiseffect suppresses the pressing of an electrolytic solution out of thenegative-electrode active material layer 52 when thenonaqueous-electrolyte secondary battery 10 is charged or discharged.

Furthermore, a stress applied to the separator 38 d by the expansion andcontraction of the negative-electrode active material layer 52 isabsorbed by the elastic body 40 having a lower compression modulus thanthe separator 38 d. This suppresses deformation of the separator 38 dand improves the retainability of an electrolytic solution in theelectrode body 38. Hence, an increase in resistance is suppressed duringhigh-rate charge and discharge.

A compression modulus is calculated by dividing, when a predeterminedload is applied to a sample in the thickness direction, the deformationamount of the sample in the thickness direction by a compression areaand then multiplying the deformation amount by the thickness of thesample as expressed by the following formula: A compression modulus(MPa)=load (N)/compression area (mm²)×(sample deformation amount(mm)/sample thickness (mm)). In the measurement of the compressionmodulus of the negative-electrode active material layer 52, thecompression modulus of the negative-electrode current collector 50 ismeasured, the compression modulus of sample 1 in which the first layer52 a is formed on the negative-electrode current collector 50 ismeasured, and the compression modulus of sample 2 in which the secondlayer 52 b is formed on the first layer 52 a on the negative-electrodecurrent collector 50 is measured. Based on the compression moduli of thenegative-electrode current collector 50 and sample 1, the compressionmodulus of the first layer 52 a is calculated. Based on the compressionmoduli of sample 1 and sample 2, the compression modulus of the secondlayer 52 b is calculated. When the compression moduli of the first layer52 a and the second layer 52 b are determined from the produced negativeelectrode 38 b, the compression modulus of the negative electrode 38 bis measured, the compression modulus of sample 1 in which the secondlayer 52 b is removed from the negative electrode is measured, and thenthe compression modulus of the negative-electrode current collector 50is measured. Based on the measured compression moduli, the compressionmoduli of the first layer 52 a and the second layer 52 b can bedetermined.

FIG. 5 is a schematic cross-sectional view of the elastic bodiesdisposed in the housing. When the elastic bodies 40 are placed with thenonaqueous-electrolyte secondary batteries 10 as described above, theelastic bodies 40 are not always placed outside the housing 13. Theelastic bodies 40 may be placed inside the housing 13. The elasticbodies 40 in FIG. 5 are disposed on both ends of the electrode body 38in the stacking direction (first direction X) of the electrode bodies38. The elastic body 40 is interposed between the inner wall of thehousing 13 and the electrode body 38.

When the electrode body 38 is expanded by, for example, the charge anddischarge of the nonaqueous-electrolyte secondary battery 10, a loadapplied outward in the first direction X is generated in the electrodebody 38. In other words, the elastic bodies 40 placed in the housing 13receive a load from the electrode body 38 in the first direction X (thestacking direction of the electrode body). The same effect can beobtained if the compression moduli satisfy the relationship of the firstlayer 52 a>the second layer 52 b>the separator 38 d>the elastic body 40.

The elastic bodies 40 in the housing 13 may be placed at any positionsas long as a load can be received from the electrode body 38 in thestacking direction of the electrode body 38. For example, in the case ofthe electrode body 38 of the cylindrical winding type in FIG. 6, theelastic body 40 may be placed in a winding core 39 of the electrode body38 of the cylindrical winding type. The stacking direction of theelectrode body 38 of the cylindrical winding type is a radial direction(R) of the electrode body 38. As the electrode body 38 expands orcontracts, a load is generated in the electrode body 38 in the stackingdirection (the radial direction (R) of the electrode body 38) of theelectrode body 38, and the elastic body 40 in the winding core 39receives the load in the stacking direction of the electrode body 38. Ifthe multiple electrode bodies 38 are placed in the housing 13, which isnot illustrated, the elastic body 40 may be disposed between theadjacent electrode bodies 38. Also in the case of the flat winding type,the electrode body may be placed at the center of the electrode body.

The negative electrode 38 b is produced by using, for example, a firstnegative-electrode mixture slurry containing negative-electrode activematerial particles P1 and a binder, and a second negative-electrodemixture slurry containing negative-electrode active material particlesP2 and a binder. Specifically, the surface of the negative-electrodecurrent collector 50 is coated with the first negative-electrode mixtureslurry, and the coating is dried. Thereafter, the secondnegative-electrode mixture slurry is applied onto a first coating formedby the first negative-electrode mixture slurry, and a second coating isdried, obtaining the negative electrode 38 b in which thenegative-electrode active material layer 52 including the first layer 52a and the second layer 52 b is formed on the negative-electrode currentcollector 50. A method of adjusting the compression moduli of the firstlayer 52 a and the second layer 52 b is, for example, a method ofrolling the formed first coating and the formed second coating andadjusting the roll forces of the coatings. Alternatively, thecompression moduli can be also adjusted by changing, for example, thematerial properties and physical properties of negative-electrode activematerials used for the first layer 52 a and the second layer 52 b. Theadjustment of compression moduli of the layers is not limited to theforegoing adjustment.

In the present embodiment, the negative-electrode active materialparticles P1 constituting the first layer 52 a near thenegative-electrode current collector include graphite particles and atleast one Si particle selected from the group consisting of lithiumsilicate particles and silicon carbon composite particles. The graphiteparticles contained in the first layer 52 a have a BET specific surfacearea of 1 to 2.5 m²/g. The content of the Si particles in the firstlayer 52 a is 6 mass % to 13 mass % relative to the total amount of thenegative-electrode active material layer 52.

Lithium silicate particles may be any conventionally known particles aslong as lithium ions can be reversibly occluded and released. Forexample, lithium silicate particles expressed by a general formulaLi_(x)SiO_(y) (0<x≤4, 0<y≤4) may be used. Lithium silicate particles maybe composited with, for example, silicon particles. Composite particlesincluding, for example, a lithium silicate phase expressed by a generalformula Li_(x)SiO_(y) (0<x≤4, 0<y≤4) and silicon particles dispersed inthe lithium silicate phase may be used. The lithium silicate phase is anaggregate of lithium silicate particles. Alternatively, compositeparticles including, for example, a silicon phase, and lithium silicateparticles that are dispersed in the silicon phase and are expressed by ageneral formula Li_(x)SiO_(y) (0<x≤4, 0<y≤4) may be used. The siliconphase is an aggregate of silicon particles. The lithium silicateparticles preferably have an Li composition of Li_(1.0)SiO toLi_(1.7)SiO, a reversible capacitance of 1600 mAh/g to 1700 mAh/g, andinitial efficiency (initial discharged capacity/initial chargedcapacity) of about 82% and 86%.

Silicon carbon composite particles may be any conventionally knownparticles, as long as lithium ions can be reversibly occluded andreleased. For example, silicon carbon composite particles expressed by ageneral formula Si_(x)Cl_(y) (0<x≤1, 0<y≤1) may be used. Silicon carboncomposite particles may be composite particles of, for example, siliconparticles and carbon. Nanosized silicon may be embedded into a carbonmatrix. Some silicon particles may be oxidized. Carbon may have a lowdegree of crystallinity at a low heat-treatment temperature or have ahigh degree of crystallinity like graphite. For example, the range ofthe composition of Si_(x)Cl_(y) is preferably expressed as 0.3≤x≤0.45and 0.7≤y≤0.55. The reversible capacitance is preferably 1300 mAh/g to1900 mAh/g, and the initial efficiency (initial dischargedcapacity/initial charged capacity) is preferably about 90% to 95%.

As described above, graphite particles contained in the first layer 52 anear the negative-electrode current collector have a BET specificsurface area of 1 m²/g to 2.5 m²/g and the content of the Si particlesin the first layer 52 a near the negative-electrode current collector is6 mass % to 13 mass % relative to the total amount of thenegative-electrode active material layer 52, thereby suppressing areduction in capacity recovery rate in the nonaqueous-electrolytesecondary battery after high-temperature storage. This mechanism is notsufficiently clarified. It is assumed that the use of the configurationsuppresses the reductive decomposition of an electrolytic solutionduring the high-temperature storage of the nonaqueous-electrolytesecondary battery so as to suppress a reduction in capacity recoveryrate after the high-temperature storage. If the BET specific surfacearea of graphite particles exceeds 2.5 m²/g and the content of the Siparticles exceeds 13 mass %, the reductive decomposition of theelectrolytic solution is not sufficiently suppressed during thehigh-temperature storage of the nonaqueous-electrolyte secondarybattery, thereby preventing a reduction in capacity recovery rate frombeing sufficiently suppressed after the high-temperature storage. It isalso assumed that even if the BET specific surface area of graphiteparticles is smaller than 1 m²/g or the content of the Si material isless than 6 mass %, the effect of suppressing a reduction in capacityrecovery rate after the high-temperature storage can be obtained.However, the capacity of the nonaqueous-electrolyte secondary batterymay be reduced and thus the BET specific surface area of graphiteparticles and the content of the Si material do not correspond to thescope of the present disclosure.

The graphite particles contained in the first layer 52 a may have a BETspecific surface area of 1 to 2.5 m²/g, preferably 1 to 2.2 m²/g. Thecontent of the Si particles in the first layer 52 a may be 6 mass % to13 mass %, preferably 6 mass % to 10 mass %, relative to the totalamount of the negative-electrode active material layer 52.

The graphite particles contained in the first layer 52 a preferablyinclude two kinds of graphite particles having different averageparticle diameters. Specifically, graphite particles (A) preferably havea larger average particle diameter than graphite particles (B), and theratio of the average particle diameter of graphite particles (B) to thatof graphite particles (A) is preferably 0.3 to 0.5. This increases, forexample, the filling density of the first layer 52 a, allowing thenonaqueous-electrolyte secondary battery to have a larger capacity. Theaverage particle diameter means a volume average particle diameter witha volume integrated value of 50% in a particle size distributionobtained by laser diffraction scattering.

The graphite particles contained in the first layer 52 a preferablyinclude two kinds of graphite particles having different particlecompressive strengths. Specifically, graphite particles (C) preferablyhave a higher particle compressive strength than graphite particles (D),the ratio of the particle compressive strength of graphite particles (D)to that of graphite particles (C) is preferably 0.2 to 0.6, and graphiteparticles (D) preferably have a particle compressive strength of 10 MPato 35 MPa. This increases, for example, the filling density of the firstlayer 52 a, thereby allowing the nonaqueous-electrolyte secondarybattery to have a larger capacity. The particle compressive strength canbe measured by, for example, a micro compression tester MCT-211 byShimadzu Corporation.

Specifically, graphite particles are placed on a stage, the center of aparticle is targeted under a microscope, a particle with a diameter of20 μm is pressed with a load rate of 2.665 mN/sec, and the strength ofthe particle is measured with N=10 when the particle is broken. The meanvalue of strengths is defined as a particle compressive strength.

The graphite particles contained in the first layer 52 a may beparticles of, for example, natural graphite or artificial graphite. Forexample, the content of graphite particles is preferably 85 mass % orgreater, preferably 90 mass % or greater relative to the total amount ofthe first layer 52 a. The negative-electrode active material particlesP1 constituting the first layer 52 a may contain negative-electrodeactive material particles other than graphite particles and the Siparticles without lessening the effect of the present disclosure.

The negative-electrode active material particles P2 constituting thesecond layer 52 b may be any material particles capable of reversiblyoccluding and releasing lithium ions. For example, the particles maycontain carbon materials such as natural graphite, artificial graphite,non-graphitizable carbon, and graphitizable carbon; surface-modifiedcarbon materials that are carbon materials covered with amorphous carbonfilms; metals alloyed with lithium, e.g., silicon (Si) and tin (Sn), oralloys containing metallic elements such as Si and Sn; or compoundscontaining metallic elements such as Si and Sn. However, if the secondlayer 52 b near the surface contains a large amount of compounds otherthan carbon materials, such as Si compounds of the lithium silicateparticles and the silicon carbon composite particles or Sn compounds,the reductive decomposition of an electrolytic solution is likely tooccur during the high-temperature storage of the nonaqueous-electrolytesecondary battery. Thus, the second layer 52 b desirably contains fewcompounds other than carbon materials. For example, compounds other thancarbon materials preferably account for at most 1 mass % relative to thetotal amount of the negative-electrode active material layer 52.

The first layer 52 a preferably contains 0.01 mass % to 0.4 mass % of acarbon nanotube having one to five graphene sheets and more preferablycontains 0.02 mass % to 0.3 mass % of the carbon nanotube, in view ofsuppression of deterioration of charge and discharge cyclecharacteristics regarding the nonaqueous-electrolyte secondary battery,for example. In this case, a graphene sheet means a layer in which thecarbon atoms of an sp2 hybridized orbital making up graphite crystalsare located at the apexes of a regular hexagon. A carbon nanotube havinga single graphene sheet is generally called a single-walled carbonnanotube (SWCNT) with a carbon nanostructure in which a single graphenesheet constitutes a single cylindrical shape. A carbon nanotube havingat least two graphene sheets is generally called a multi-walled carbonnanotube with a carbon nanostructure in which multiple graphene sheetsare concentrically stacked to constitute a single cylindrical shape. Thefirst layer 52 a may include a carbon nanotube having at least sixgraphene sheets. The first layer 52 a preferably includes few carbonnanotubes, in consideration of suppression of a reduction in capacity inthe charge and discharge cycle. The content of a carbon nanotube ispreferably at most 0.01 mass % with respect to the first layer 52 a. Thesecond layer 52 b may also contain a carbon nanotube (single-walled ormulti-walled).

The second layer 52 b preferably has a larger porosity rate than thefirst layer 52 a. This may increase the penetration of an electrolyticsolution into the negative-electrode active material layer 52 andcontribute to, for example, suppression of an increase in resistanceduring high-rate charge and discharge, or suppression of a reduction incapacity in a charge and discharge cycle. The porosity rates of thefirst layer 52 a and the second layer 52 b are two-dimensional values,each being determined from the area ratio of pores between particles ineach layer relative to the cross-sectional area of each layer. Forexample, the porosity rates are determined by the following steps.

(1) The negative electrode is partially cut, and then the negativeelectrode is processed by an ion milling device (e.g., IM4000 by HitachiHigh-Tech Corporation) so as to expose the cross section of thenegative-electrode active material layer 52.

(2) A reflection electron image of the cross section of the first layer52 a in the exposed negative-electrode active material layer 52 iscaptured by using a scanning electron microscope.

(3) The cross-sectional image obtained thus is captured by a computerand is binarized using image analysis software (e.g., ImageJ by theNational Institutes of Health), obtaining a binary image in which thecross sections of particles in the cross-sectional image are black andpores between particles and pores in particles are white.

(4) The area of pores between particles in a measurement range (50 μm×50μm) is calculated from a binary image. The cross-sectional area (2500μm²=50 μm×50 μm) of the first layer 52 a is set as the measurementrange, and the porosity rate of the first layer 52 a (the area of poresbetween particles×100/the cross-sectional area of the negative-electrodeactive material layer 52) is calculated from the calculated area ofpores between particles.

The particle-internal porosity rate of the negative-electrode activematerial particles P2 and the porosity rate of the second layer 52 b aresimilarly measured.

A method of adjusting the porosity rates of the first layer 52 a and thesecond layer 52 b is, for example, a method of adjusting roll forcesapplied to the first coating and the second coating during the formationof the negative-electrode active material layer 52.

The compression modulus of the second layer 52 b is preferably at least1.2 times and more preferably at least twice the compression modulus ofthe second layer 52 b. The satisfaction of the range may suppress, forexample, an increase in resistance during high-rate charge anddischarge.

The negative-electrode active material layer 52 has a thickness of, forexample, 40 μm to 120 μm, preferably 50 μm to 90 μm on one side of thenegative-electrode current collector 50. The thickness of thenegative-electrode active material layer 52 is measured from across-sectional image of the negative electrode 38 b, the image beingcaptured by a scanning electron microscope (SEM).

For the negative-electrode current collector 50, a metal leaf that isstable in the potential range of the negative electrode 38 b or a filmhaving a metallic surface layer is used. For example, materials such ascopper may be used.

The positive electrode 38 a includes, for example, a positive-electrodecurrent collector and a positive-electrode active material layer formedon the positive-electrode current collector. For the positive-electrodecurrent collector, a metal leaf that is stable in the potential range ofthe positive electrode or a film having a metallic surface layer isused. For example, aluminum or an aluminum alloy may be used. Thepositive-electrode active material preferably containspositive-electrode active material particles, a conductive material, anda binder and is preferably provided on both sides of thepositive-electrode current collector. The positive electrode 38 a can beproduced by, for example, applying a coating of positive-electrodemixture slurry containing a positive-electrode active material, aconductive material, and a binder to the positive-electrode currentcollector, drying the coating, and then compressing the coating into apositive-electrode active material layer on each side of thepositive-electrode current collector.

The positive-electrode active material is, for example, alithium-transition metal composite oxide. A lithium-transition metalcomposite oxide contains metallic elements such as Ni, Co, Mn, Al, B,Mg, Ti, V, Cr, Fe, Cu, Zn, Ga, Sr, Zr, Nb, In, Sn, Ta, and W. From amongthe metallic elements, at least one of Ni, Co, and Mn is preferablycontained. A composite oxide is, for example, a lithium-transition metalcomposite oxide containing Ni, Co, and Mn or a lithium-transition metalcomposite oxide containing Ni, Co, and Al.

The separator 38 d is, for example, a porous sheet with ion permeationand insulation. Specific examples of a porous sheet include amicroporous thin film, a woven fabric, and a nonwoven fabric. Theseparator 38 d is may be made of materials including olefin resins suchas polyethylene and polypropylene and cellulose. The separator 38 d maybe a stack including a cellulose fiber layer and a thermoplastic-resinfiber layer containing olefin resin. Alternatively, the separator 38 dmay be a multilayer separator including a polyethylene layer and apolypropylene layer. The surface of the separator 38 d may be coatedwith materials such as aramid resin and ceramic.

The separator 38 d may have any compression modulus lower than that ofthe first layer 52 a of the negative-electrode active material layer 52.For example, the compression modulus is preferably 0.1 to 0.6 times,more preferably 0.15 to 0.5 times the compression modulus of the firstlayer 52 a in view of effective suppression of an increase in resistanceduring high-rate charge and discharge. The compression modulus of theseparator 38 d is adjusted by controlling, for example, the selection ofmaterials, a porosity rate, and a pore size.

The electrolytic solution is, for example, a nonaqueous electrolyticsolution containing a supporting electrolyte in an organic solvent(nonaqueous solvent). The nonaqueous solvent may be a solventcontaining, for example, esters, ethers, nitriles, or amides, or a mixedsolvent containing at least two kinds of these compounds. The supportingelectrolyte is, for example, a lithium salt such as LiPF₆.

The materials of the elastic body 40 include, for example, thermosettingelastomers such as natural rubber, polyurethane rubber, silicone rubber,and fluorocarbon rubber and thermoplastic elastomers such aspolystyrene, olefin, urethane, polyester, and polyamide. These materialsmay be foamed materials. Moreover, a heat insulating material thatsupports porous materials such as silica xerogel may be used.

The elastic body 40 may have any compression modulus lower than that ofthe separator 38 d. For example, the compression modulus is preferably120 MPa or less and is more preferably 80 MPa or less in view ofeffective suppression of an increase in resistance during high-ratecharge and discharge.

The elastic body 40 may have a constant compression modulus in one planebut may vary in deformability in the plane as will be described below.

FIG. 7 is a schematic perspective view illustrating an example of theelastic body. The elastic body 40 in FIG. 7 has a soft portion 44 andhard portions 42. The hard portions 42 are placed on the outer edges ofthe elastic body 40 with respect to the soft portion 44. The elasticbody 40 in FIG. 7 has a structure in which the hard portions 42 aredisposed on both ends in the second direction Y and the soft portion 44is disposed between the two hard portions 42. The soft portion 44 ispreferably disposed so as to overlap the center of the long lateralfaces of the housing 13 and the center of the electrode body 38 in thefirst direction X. The hard portions 42 are preferably disposed so as tooverlap the outer edges of the long lateral faces of the housing 13 andthe outer edge of the electrode body 38 in the first direction X.

As described above, the nonaqueous-electrolyte secondary battery 10 isexpanded mainly by the expansion of the electrode body 38. The expansionof the electrode body 38 increases toward the center. Specifically, thedisplacement of the electrode body 38 increases toward the center in thefirst direction X and decreases from the center toward the outer edge.According to the displacement of the electrode body 38, the displacementof the nonaqueous-electrolyte secondary battery 10 increases toward thecenter of the long lateral face of the housing 13 in the first directionX and decreases from the center toward the outer edge of the longlateral face of the housing 13. Thus, if the elastic body 40 in FIG. 7is placed in the housing 13, the elastic body 40 can receive, with thesoft portion 44, a large load generated by a large displacement of theelectrode body 38 and receive, with the hard portions 42, a small loadgenerated by a small displacement of the electrode body 38. If theelastic body 40 in FIG. 7 is placed outside the housing 13, the elasticbody 40 can receive, with the soft portion 44, a large load generated bya large displacement of the nonaqueous-electrolyte secondary battery 10and receive, with the hard portions 42, a small load generated by asmall displacement of the nonaqueous-electrolyte secondary battery 10.

The elastic body 40 in FIG. 7 has a recessed portion 46 in the firstdirection X. A non-recessed portion adjacent to the recessed portion 46can be partially displaced to the recessed portion 46 when receiving aload from the nonaqueous-electrolyte secondary battery 10 or theelectrode body 38. Thus, the provision of the recessed portion 46 canfacilitate deformation of the non-recessed portion. In thisconfiguration, in order to make the soft portion 44 more deformable thanthe hard portions 42, the area ratio of the recessed portion 46 to thearea of the soft portion 44 is preferably larger than the area ratio ofthe recessed portion 46 to the area of the hard portions 42 in the firstdirection X. On the elastic body 40 in FIG. 7, the recessed portion 46is disposed only in the soft portion 44. The recessed portion 46 may bedisposed in the hard portions 42.

The recessed portion 46 includes a core portion 46 a and a plurality oflinear portions 46 b. The core portion 46 a is shaped like a circledisposed at the center of the elastic body 40 in the first direction X.The linear portions 46 b are radially extended from the core portion 46a. Since the linear portions 46 b are radially extended, the ratio ofthe linear portions 46 b increases toward the core portion 46 a and thenon-recessed portions decreases toward the core portion 46 a. Thus, thedeformability of the non-recessed portions increases near the coreportion 46 a.

The elastic body 40 may have a plurality of through holes penetratingthe elastic body 40 in the first direction X, instead of or along withthe recessed portion 46. The through holes are not illustrated. Theprovision of the through holes can facilitate deformation ofnon-penetrating portions. Hence, in order to make the soft portion 44more deformable than the hard portions 42, the area ratio of the throughholes to the area of the soft portion 44 is preferably larger than thearea ratio of the through holes to the area of the hard portions 42 inthe first direction X.

Another example of the elastic body will be described below.

FIG. 8 is a partial schematic cross-sectional view of the elastic bodydisposed between the electrode body and the housing. The elastic body 40receives a load from the electrode body 38 in the stacking direction(first direction X) of the electrode body 38. The elastic body 40includes a substrate 42 a where the hard portions 42 havingpredetermined hardness are formed, and the soft portion 44 that issofter than the hard portion 42. The hard portion 42 is a projectingportion that projects from the substrate 42 a toward the electrode body38 and may be ruptured or plastically deformed by at least apredetermined load. The soft portion 44 is shaped like a sheet disposedbetween the substrate 42 a where the hard portions 42 are formed and theelectrode body 38 near the electrode body 38. The soft portion 44 isseparated from the electrode body 38. The soft portion 44 has throughholes 44 a at positions overlapping the hard portions 42 in the firstdirection X. The hard portion 42 is inserted into the through hole 44 a,and the tip of the hard portion 42 projects from the soft portion 44.

In response to a change of the shapes of the hard portions 42, theelastic body 40 shifts from a first state in which a load from theelectrode body 38 is received by the hard portions 42 to a second statein which the load is received by the soft portion 44. In other words, inthe elastic body 40, a load applied in the stacking direction of theelectrode body 38 by the expansion of the electrode body 38 is receivedby the hard portions 42 (first state). Thereafter, if for some reasonthe amount of expansion of the electrode body 38 increases so as toapply an excessive load to the hard portions 42, the hard portions 42 isruptured or plastically deformed, the electrode body 38 comes intocontact with the soft portion 44, and the load in the stacking directionof the electrode body 38 is received by the soft portion 44 (secondstate).

In the case of an elastic body having asperities, the compressionmodulus is calculated as follows: the compression modulus (MPa)=a load(N)/a projection area (mm²) in the planar direction of the elasticbody×(the modification (mm) of the elastic body/the thickness (mm) ofthe elastic body to a projecting portion).

EXAMPLES

The present disclosure will be further described in accordance withexamples. The present disclosure is not limited to the examples.

Example 1

[Production of a Positive Electrode]A lithium-transition metal compositeoxide expressed by the general formula LiNi_(0.82)Co_(0.15)Al_(0.03)O₂was used as a positive-electrode active material. The positive-electrodeactive material, acetylene black, and polyvinylidene fluoride were mixedwith a solid mass ratio of 97:2:1, and a positive-electrode mixtureslurry was prepared by using N-methyl-2-pyrrolidone (NMP) as adispersion medium. Subsequently, a coating of the positive-electrodemixture slurry was applied to each side of a positive-electrode currentcollector composed of aluminum foil. The coating was dried, rolled, andthen cut into a predetermined electrode size, so that a positiveelectrode was obtained with a positive-electrode active material layerformed on each side of the positive-electrode current collector.

[Preparation of a First Negative-Electrode Mixture Slurry]

Graphite particles having a BET specific surface area of 1.5 m²/g,lithium silicate particles (LiSiO), a single-walled carbon nanotube, thedispersion of styrene-butadiene rubber (SBR), and sodiumcarboxymethylcellulose (CMC-Na) were mixed at a solid mass ratio of76:24:0.01:1:1, and the first negative-electrode mixture slurry wasprepared by using water as a dispersion medium.

[Preparation of a Second Negative-Electrode Mixture Slurry]

Graphite particles having a BET specific surface area of 2.9 m²/g, thedispersion of SBR, and CMC-Na were mixed at a solid mass ratio of100:1:1.5, and the second negative-electrode mixture slurry was preparedby using water as a dispersion medium.

[Production of a Negative Electrode]

A coating of the first negative-electrode mixture slurry was applied toeach side of the negative-electrode current collector composed of copperfoil, the coating was dried and rolled, a coating of the secondnegative-electrode mixture slurry was applied onto the coating, and thecoating was dried and rolled, so that a negative-electrode activematerial layer was formed with a first layer of the firstnegative-electrode mixture slurry and a second layer of the secondnegative-electrode mixture slurry on the negative-electrode currentcollector. The negative-electrode active material layer was cut into apredetermined electrode size so as to obtain a negative electrode. Thenegative-electrode active material layer having a thickness of 160 μm(except for the negative-electrode current collector) was formed with anequal amount of application of the first and second negative-electrodemixture slurry. The content of the lithium silicate particles was 12mass % relative to the total amount of the negative-electrode activematerial layer. During the production of the negative electrode, themeasured compression moduli of the first and second layers were 750 MPaand 900 MPa.

[Preparation of an Electrolytic Solution]

Ethylene carbonate (EC), methyl ethyl carbonate (EMC), and dimethylcarbonate (DMC) were mixed at a volume ratio of 3:3:4. An electrolyticsolution was prepared by dissolving LiPF₆ at a concentration of 1.4mol/L in the mixed solvent.

[Production of the Nonaqueous-Electrolyte Secondary Battery]

Negative electrodes, separators with a compression modulus of 120 MPa,and positive electrodes were sequentially stacked to produce anelectrode body. The negative electrodes and the positive electrodes wereconnected to the positive terminal and the negative terminal and werestored in an exterior part including an aluminum laminate. After theelectrolytic solution was poured into the exterior part, the opening ofthe exterior part was sealed, so that the nonaqueous-electrolytesecondary battery was produced.

The produced nonaqueous-electrolyte secondary battery was held by a pairof elastic bodies (a urethane foam having a compression modulus of 60MPa) and was held and fixed by a pair of end plates, so that thesecondary battery module was produced.

Example 2

The secondary battery module was produced as in Example 1 except thatgraphite particles having a BET specific surface area of 1.5 m²/g,silicon carbon composite particles (Si_(0.4)C_(0.6)), a single-walledcarbon nanotube, the dispersion of styrene-butadiene rubber (SBR), andsodium carboxymethylcellulose (CMC-Na) were mixed at a solid mass ratioof 76:24:0.01:1:1.5 in the preparation of the first negative-electrodemixture slurry. The content of the silicon carbon composite particleswas 12 mass % relative to the total amount of the negative-electrodeactive material layer. During the production of the negative electrode,the measured compression moduli of the first and second layers were 700MPa and 900 MPa.

Example 3

The secondary battery module was produced as in Example 1 except thatgraphite particles having a BET specific surface area of 1.5 m²/g,lithium silicate particles (LiSiO), a single-walled carbon nanotube, thedispersion of styrene-butadiene rubber (SBR), and sodiumcarboxymethylcellulose (CMC-Na) were mixed at a solid mass ratio of76:24:0.4:1:1.5 in the preparation of the first negative-electrodemixture slurry. The content of the lithium silicate particles was 12mass % relative to the total amount of the negative-electrode activematerial layer. During the production of the negative electrode, themeasured compression moduli of the first and second layers were 750 MPaand 900 MPa.

Example 4

The secondary battery module was produced as in Example 1 except thatmixed graphite particles prepared by mixing graphite particles having anaverage particle diameter of 8 μm and graphite particles having anaverage particle diameter of 18 μm at a mass ratio of 4:6, lithiumsilicate particles (LiSiO), a single-walled carbon nanotube, thedispersion of styrene-butadiene rubber (SBR), and sodiumcarboxymethylcellulose (CMC-Na) were mixed with a solid mass ratio of76:24:0.01:1:1.5 in the preparation of the first negative-electrodemixture slurry. The measured BET specific surface area of the mixedgraphite was 2.5 m²/g. The content of the lithium silicate particles was12 mass % relative to the total amount of the negative-electrode activematerial layer. During the production of the negative electrode, themeasured compression moduli of the first and second layers were 700 MPaand 900 MPa.

Example 5

The secondary battery module was produced as in Example 1 except thatmixed graphite particles prepared by mixing graphite particles having aparticle compressive strength of 60 MPa and graphite particles having aparticle compressive strength of 15 MPa at a mass ratio of 6:4, lithiumsilicate particles (LiSiO), a single-walled carbon nanotube, thedispersion of styrene-butadiene rubber (SBR), and sodiumcarboxymethylcellulose (CMC-Na) were mixed at a solid mass ratio of76:24:0.4:1:1.5 in the preparation of the first negative-electrodemixture slurry. The measured BET specific surface area of the mixedgraphite was 2.5 m²/g. The content of the lithium silicate particles was12 mass % relative to the total amount of the negative-electrode activematerial layer. During the production of the negative electrode, themeasured compression moduli of the first and second layers were 650 MPaand 900 MPa.

Comparative Example 1

The nonaqueous-electrolyte secondary battery was produced as in Example1 except that graphite particles having a BET specific surface area of4.5 m²/g, lithium silicate particles (LiSiO), a multi-walled carbonnanotube having five graphene sheets, the dispersion ofstyrene-butadiene rubber (SBR), and sodium carboxymethylcellulose(CMC-Na) were mixed at a solid mass ratio of 76:24:1:1:1.5 in thepreparation of the first negative-electrode mixture slurry. The contentof the lithium silicate particles was 12 mass % relative to the totalamount of the negative-electrode active material layer. During theproduction of the negative electrode, the measured compression moduli ofthe first and second layers were 550 MPa and 900 MPa.

The produced nonaqueous-electrolyte secondary battery was held and fixedby a pair of end plates, so that the secondary battery module wasproduced. In other words, the elastic body was not disposed between thenonaqueous-electrolyte secondary battery and the end plate.

Comparative Example 2

The nonaqueous-electrolyte secondary battery produced in ComparativeExample 1 was held by a pair of elastic bodies (a urethane foam having acompression modulus of 60 MPa) and was held and fixed by a pair of endplates, so that the secondary battery module was produced.

[Measurement of an Initial Resistance (IV Resistance)]

The initial resistances of the secondary battery modules according tothe examples and the comparative examples were measured under thefollowing conditions: The secondary battery module adjusted in acharging state of SOC 60% was subjected to constant current discharge ata temperature of 25° C. at 2 C rate for ten seconds, so that a voltagedrop (V) was calculated. The value (V) of the voltage drop was dividedby a corresponding current value (I) to calculate an IV resistance (mΩ),and then the mean value of the resistance was determined as an initialresistance.

[High-Rate Charge and Discharge Test]

Subsequently, for the secondary battery modules according to theexamples and the comparative examples, a charge and discharge cycle testwas conducted such that ten cycles of charge and discharge were repeatedat a temperature of 25° C. After the cycle test, a resistance increaserate was measured. In one cycle of the charge and discharge cycle test,constant current charge was performed at a charge rate of 1.5 C for 4300seconds, the charge was suspended for ten seconds, constant currentdischarge was performed at a discharge rate of 1.5 C for 4300 seconds,and then the discharge was suspended for ten seconds. Subsequently, theresistances (IV resistances) of the secondary battery modules after thecharge and discharge cycle test were measured by the same method as themeasurement of the initial resistance, and a resistance increase ratewas measured. The test was repeated until the rate of increase reached200%. Thereafter, the effect of suppressing an increase in resistanceduring high-rate charge and discharge was evaluated based on thefollowing evaluation criteria:

◯: The number of cycles necessary for obtaining a resistance increaserate exceeding 200% is at least 80 cycles

x: The number of cycles necessary for obtaining a resistance increaserate exceeding 200% is less than 80 cycles

[Initial Discharged-Capacity Measurement Test]

For the secondary battery modules of the examples and the comparativeexamples in an initial state, constant current charge was performeduntil a battery voltage reached 4.2 V at a constant current value of ⅓A, constant current discharge was performed until the battery voltagereached 2.5 V at a constant current value of ⅓ A, and then an initialdischarged capacity was measured.

[High-Temperature Storage Test]

For the secondary battery modules of the examples and the comparativeexamples after the initial discharged-capacity measurement test,constant current charge was performed until a battery voltage reached4.2 V at a constant current value of ⅓ A, and then each battery wasstored in a thermostat at 60° C. for sixty days. After sixty days, eachbattery was collected, and then a discharged capacity after thehigh-temperature storage was measured like an initial capacity. Thedischarged capacity after the high-temperature storage was divided bythe initial discharged capacity, so that a capacity recovery rate wascalculated.

Table 1 shows the test results of the examples and the comparativeexamples.

TABLE 11 NEGATIVE-ELECTRODE ACTIVE MATERIAL LAYER FIRST LAYER CARBONSECOND LAYER NANOTUBE GRAPHITE GRAPHITE THE PARTICLES COMPRESSIONPARTICLE COMPRESSION NUMBER BET MODULUS BET MODULUS OF (m²/g) (MPa)(m²/g) (MPa) LAYERS CONTENT EXAMPLE 1 2.9 900 1.5 750 1 0.01 wt %EXAMPLE 2 2.9 900 1.5 750 1 0.01 wt % EXAMPLE 3 2.9 900 1.5 750 1  0.4wt % EXAMPLE 4 2.9 900 2.5 700 1  0.4 wt % (AVERAGE PARTICLE DIAMETER 8um, 18 um) EXAMPLE 5 2.9 900 2.5 650 1  0.4 wt % (COMPRESSIVE STRENGTH60 MPa, 15 MPa) COMPARATIVE 2.9 900 4.5 550 5   1 wt % EXAMPLE 1COMPARATIVE 2.9 900 4.5 550 5   1 wt % EXAMPLE 2 NEGATIVE- TEST RESULTELECTRODE EFFECT OF ACTIVE SUPPRESSING MATERIAL INCREASE IN CAPACITYLAYER RESISTANCE RECOVERY FIRST LAYER SEPARATOR ELASTIC BODY DURINGHIGH- RATE AFTER CONTENT COMPRESSION COMPRESSION RATE CHARGE HIGH- OF SiMODULUS MODULUS AND TEMPERATURE PARTICLES (MPa) (MPa) DISCHARGE STORAGE(%) EXAMPLE 1 LiSi0 120 60 O 91 12 wt % EXAMPLE 2 Si_(0.4)C_(0.6) 120 60O 89 12 wt % EXAMPLE 3 LiSi0 120 60 O 89 12 wt % EXAMPLE 4 LiSi0 120 60O 89 12 wt % EXAMPLE 5 LiSi0 120 60 O 89 12 wt % COMPARATIVE LiSi0 120 0X 87 EXAMPLE 1 12 wt % COMPARATIVE LiSi0 120 60 O 80 EXAMPLE 2 12 wt %

According to Examples 1 to 5 in which a compression modulus satisfiesthe relationship of the second layer near the surface>the first layernear the negative-electrode current collector>the separator>the elasticbody, graphite particles contained in the first layer have a BETspecific surface area of 1 to 2.5 m²/g, and the first layer contains 12mass % of Si particles (lithium silicate particles or SiC particles), sothat an increase in resistance during high-rate charge and discharge anda reduction in capacity recovery rate after the high-temperature storageare suppressed as compared with Comparative Examples 1 and 2 that do notsatisfy the foregoing requirements.

REFERENCE SIGNS LIST

-   1 Secondary battery module-   2 Stack-   4 End plate-   6 Locking member-   8 Cooling plate-   10 Nonaqueous-electrolyte secondary battery-   12 Insulating spacer-   13 Housing-   14 Outer can-   16 Sealing plate-   18 Output terminal-   38 Electrode body-   38 a Positive electrode-   38 b Negative electrode-   38 d Separator-   39 Winding core-   40 Elastic body-   42 Hard portion-   42 a Substrate-   44 soft portion-   44 a Through hole-   46 Recessed portion-   46 a Core portion-   46 b Linear portion-   50 Negative-electrode current collector-   52 Negative-electrode active material layer-   52 a First layer-   52 b Second layer

1. A secondary battery module comprising: at least onenonaqueous-electrolyte secondary battery, and an elastic body that isplaced with the nonaqueous-electrolyte secondary battery and receives aload from the nonaqueous-electrolyte secondary battery in a placementdirection of the elastic body, wherein the nonaqueous-electrolytesecondary battery includes an electrode body in which a positiveelectrode, a negative electrode, and a separator disposed between thepositive electrode and the negative electrode are stacked, and a housingaccommodating the electrode body, the negative electrode includes anegative-electrode current collector, and a negative-electrode activematerial layer that is formed on the negative-electrode currentcollector and contains negative-electrode active material particles, thenegative-electrode active material layer including a first layer formedon the negative-electrode current collector, and a second layer that isformed on the first layer and has a higher compression modulus than thefirst layer, the separator has a lower compression modulus than thefirst layer, the elastic body has a lower compression modulus than theseparator, the negative-electrode active material particles contained inthe first layer include graphite particles and at least one Si particleselected from the group consisting of lithium silicate particles andsilicon carbon composite particles, the graphite particles contained inthe first layer have a BET specific surface area of 1 to 2.5 m²/g, and acontent of the Si particles is 6 mass % to 13 mass % relative to a totalamount of the negative-electrode active material layer.
 2. The secondarybattery module according to claim 1, wherein the first layer contains0.01 mass % to 0.4 mass % of a carbon nanotube having one to fivegraphene sheets.
 3. The secondary battery module according to claim 1,wherein the graphite particles contained in the first layer include twokinds of graphite particles having different average particle diameters,graphite particles (A) have a larger average particle diameter thangraphite particles (B), and a ratio of the average particle diameter ofgraphite particles (B) to the average particle diameter of graphiteparticles (A) is 0.3 to 0.5.
 4. The secondary battery module accordingto claim 1, wherein the graphite particles contained in the first layerinclude two kinds of graphite particles having different particlecompressive strengths, graphite particles (C) have a larger particlecompressive strength than graphite particles (D), a ratio of theparticle compressive strength of graphite particles (D) to the particlecompressive strength of graphite particles (C) is 0.2 to 0.6, andgraphite particles (D) have a particle compressive strength of 10 MPa 35MPa.
 5. The secondary battery module according to claim 1, wherein thesecond layer has a higher porosity rate than the first layer.
 6. Thesecondary battery module according to claim 1, wherein the elastic bodyhas a compression modulus of at most 120 MPa.
 7. Anonaqueous-electrolyte secondary battery comprising: an electrode bodyin which a positive electrode, a negative electrode, and a separatordisposed between the positive electrode and the negative electrode arestacked, an elastic body configured to receive a load from the electrodebody in a stacking direction of the electrode body, and a housingaccommodating the electrode body and the elastic body, wherein thenegative electrode includes a negative-electrode current collector, anda negative-electrode active material layer that is formed on thenegative-electrode current collector and contains negative-electrodeactive material particles, the negative-electrode active material layerincluding a first layer formed on the negative-electrode currentcollector and a second layer that is formed on the first layer and has ahigher compression modulus than the first layer, the separator has alower compression modulus than the first layer, the elastic body has alower compression modulus than the separator, the negative-electrodeactive material particles contained in the first layer include graphiteparticles and at least one Si particle selected from the groupconsisting of lithium silicate particles and silicon carbon compositeparticles, the graphite particles contained in the first layer have aBET specific surface area of 1 to 2.5 m²/g, and a content of the Siparticles is 6 mass % to 13 mass % relative to a total amount of thenegative-electrode active material layer.